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Merck
CN

36199

Supelco

Tridemorph

PESTANAL®, analytical standard

Synonym(s):

2,6-Dimethyl-4-tridecylmorpholine

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About This Item

Empirical Formula (Hill Notation):
C19H39NO
CAS Number:
24602-86-6
Molecular Weight:
297.52
EC Number:
246-347-3
MDL number:
MFCD00055522
UNSPSC Code:
41116107
PubChem Substance ID:
329755340
NACRES:
NA.24

Key Documents

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grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

CCCCCCCCCCCCCN1CC(C)OC(C)C1

InChI

1S/C19H39NO/c1-4-5-6-7-8-9-10-11-12-13-14-15-20-16-18(2)21-19(3)17-20/h18-19H,4-17H2,1-3H3

InChI key

YTOPFCCWCSOHFV-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - Skin Irrit. 2

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCBW9105

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Yandu Lu et al.
mSystems, 5(5) (2020-10-01)
Cnidarians cannot synthesize sterols (which play essential roles in growth and development) de novo but often use sterols acquired from endosymbiotic dinoflagellates. While sterol availability can impact the mutualistic interaction between coral host and algal symbiont, the biosynthetic pathways (in
T Zamora et al.
Journal of chromatography. A, 1045(1-2), 137-143 (2004-09-24)
A rapid and sensitive liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS-MS) method for the determination of tridemorph and other pre- and post-harvest fungicides (carbendazim, thiabendazole, imazalil, propiconazole and bitertanol) in banana and orange samples has been developed and validated. The sample
A Rahier et al.
Biochemical Society transactions, 11(5), 537-543 (1983-10-01)
25-Azacycloartanol (I), 2-aza-2-dihydrosqualene (II) and Tridemorph (2,6-dimethyl-N-tridecylmorpholine) (III) are potent inhibitors of higher plant sterol biosynthesis. The first two molecules have been designed using rational enzymological concepts. I, II and III were shown to inhibit the S-adenosyl-L-methionine: cycloartenol C-24-methyltransferase, the
Ali Mohebbi et al.
Journal of chromatography. A, 1625, 461340-461340 (2020-07-28)
In this study, a magnetized polyethylene composite has been prepared using ball milling procedure and employed as an efficient sorbent in magnetic dispersive solid phase extraction combined with dispersive liquid-liquid microextraction. This method has been utilized for the extraction and
A I Shtenberg et al.
Voprosy pitaniia, (6)(6), 55-61 (1981-11-01)
Experimental studies on Wistar rats revealed that the fungicide calixin (N-tridecyl-2.6-dimethylmorpholine) has a teratogenic effect. This effect manifested in edemas, hemorrhages, hematomas, abnormal development of the brain (hydrocephalia), visceral cranium (micrognathia, cleft palate) and genitourinary system (hydronephrosis), in decreased size
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